A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585954



Internal ID21534502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78115618..78115722hg38UCSC Ensembl
chr17:76111699..76111803hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099441
SamplesNA20847
Known GenesTMC6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585954
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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